1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111186 | myopathy, lactic acidosis, and sideroblastic anemia 2 | A myopathy, lactic acidosis, and sideroblastic anemia characterized by marked phenotypic variablity in time of onset and severity of symptoms that has_material_basis_in homozyous or compound heterozygous mutation in YARS2 on 12p11.21. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:699 | mitochondrial myopathy | A myopathy that is characterized by mitochondrial dysfunction. |
